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Efficacy and safety of intravenous sufentanil administration in low-severity acute trauma as a competence of paramedics: a follow-up observational study
R. Sykora, N. Kukackova, O. Sopko, D. Peran, J. Smetana, M. Renza, M. Kukacka
Jazyk angličtina Země Německo
Typ dokumentu časopisecké články, pozorovací studie
- MeSH
- dospělí MeSH
- intravenózní podání MeSH
- klinické kompetence * MeSH
- lidé středního věku MeSH
- lidé MeSH
- management bolesti * metody MeSH
- měření bolesti MeSH
- následné studie MeSH
- opioidní analgetika * aplikace a dávkování MeSH
- prospektivní studie MeSH
- rány a poranění * komplikace diagnóza MeSH
- sufentanil * aplikace a dávkování terapeutické užití škodlivé účinky MeSH
- urgentní zdravotnické služby * metody MeSH
- zdravotničtí záchranáři * MeSH
- Check Tag
- dospělí MeSH
- lidé středního věku MeSH
- lidé MeSH
- mužské pohlaví MeSH
- ženské pohlaví MeSH
- Publikační typ
- časopisecké články MeSH
- pozorovací studie MeSH
BACKGROUND AND IMPORTANCE: In the Czech Republic, paramedics are required to consult a physician before administering intravenous opioids, which may delay effective prehospital pain management. As paramedic competencies expand in Europe, it is important to evaluate the safety and efficacy of independent opioid administration in prehospital emergency care settings. OBJECTIVES: To assess the safety and effectiveness of intravenous sufentanil administered independently by trained paramedics compared to administration following remote physician consultation in adult trauma patients. DESIGN: Prospective, single-center, observational cohort study. SETTINGS AND PARTICIPANTS: Conducted at the Emergency Medical Services of the Karlovy Vary Region between January 1 and December 31, 2024. The study included 462 adult trauma patients who were hemodynamically stable and conscious. Patients were divided into two groups: the Consultation group (physician consultation required) and the Competency group (paramedics administering independently). INTERVENTION OR EXPOSURE: Intravenous administration of sufentanil, with or without physician phone consultation. OUTCOME MEASURES AND ANALYSIS: Primary outcomes included reduction in pain (measured using the Numeric Rating Scale, NRS) and incidence of adverse events (e.g., respiratory depression, oxygen desaturation, hypotension, and antiemetic use). Statistical significance was set at p < 0.05. MAIN RESULTS: Both groups achieved similar pain reduction. The Competency group received a higher mean dose of sufentanil (9.7 ± 3.0 μg vs. 8.9 ± 2.8 μg; p = 0.006) and more frequently used non-opioid adjuvant analgesics (54% vs. 41%). Documentation of pain scores was significantly better in the Competency group (87% vs. 43%; p < 0.01). Adverse events were rare, non-serious, and comparable between groups. Antiemetics were more frequently administered in the Competency group (11% vs. 6%; p = 0.037). A minor, clinically insignificant reduction in diastolic blood pressure was observed in the Competency group. CONCLUSION: Intravenous sufentanil administered independently by trained paramedics in adult patients with lower severity trauma demonstrated safety and effectiveness comparable to administration following remote physician consultation, along with improved documentation and increased use of multimodal analgesia. Although this was a monocentric study, these observations may contribute to ongoing discussions about expanding paramedic competencies in opioid analgesia within the Czech prehospital emergency system.
Citace poskytuje Crossref.org
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